Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

  1. García-Castaño, A.
  2. Perdomo-Ramirez, A.
  3. Vall-Palomar, M.
  4. Ramos-Trujillo, E.
  5. Madariaga, L.
  6. Ariceta, G.
  7. Claverie-Martin, F.
Zeitschrift:
Molecular Genetics and Genomic Medicine

ISSN: 2324-9269

Datum der Publikation: 2020

Ausgabe: 8

Nummer: 11

Art: Artikel

DOI: 10.1002/MGG3.1475 GOOGLE SCHOLAR lock_openOpen Access editor